Author/Authors :
Zhang، نويسنده , , Li and Davis، نويسنده , , Jeffrey S. and Zelivianski، نويسنده , , Stanislav and Lin، نويسنده , , Fen-Fen and Schutte، نويسنده , , Rachel and Davis، نويسنده , , Thomas L. and Hauke، نويسنده , , Ralph and Batra، نويسنده , , Surinder K. and Lin، نويسنده , , Ming-Fong، نويسنده ,
Abstract :
We examined the efficacy of combination treatments utilizing cytotoxic drugs plus inhibitors to members of the ErbB–ERK signal pathway in human prostate cancer (PCa) LNCaP C-81 cells. Under an androgen-reduced condition, 50 nM gemcitabine caused about 40% growth suppression on C-81 cells. Simultaneous treatment of gemcitabine plus 10 μM AG825 produced 60% suppression (p < 0.03); while, 85% growth inhibition (p < 0.02) was seen if AG825 was added to gemcitabine-treated cells after a 24 h-interval. Our data thus showed that in androgen-reduced conditions, inhibition of ErbB-2 increases the cytotoxic efficacy of gemcitabine in PCa cells. This finding has significant implications in the choice of drugs for combination therapy as well as the order of administration for treating cancer patients.
Keywords :
Gemcitabine , Hormone-refractory prostate cancer , ErbB-2 inhibitor , combination therapy